Table 1.
Comparison on some main points of the principle learning models with each other and with the present model. Important note: this is not a comprehensive list but focussed on points most relevant to the present scope
Marr | New model | Albus/perceptron | Fujita/adaptive filter | |
---|---|---|---|---|
cf signal in teaching role | Yes | Yes | Yes | Yes |
Sign of cf-trained pf-PC change | LTP | LTD | LTD | LTD |
Binary or graded synaptic modification | ‘Totally modified or totally unmodified’ | Binary effect on collective transmission | Graduated | Graduated |
Function of learning | Transmission of learned patterns | Transmission of learned patterns | Learned ability to group input patterns into predefined classes | Selectively weighted transmission of pf signals to give a ‘desired response’ |
Response depends on pattern | No | No | Yes | Yes |
Functionally variable cf signature | No | No | Yes | Yes, contained in a time-varying discharge rate |
Heterogeneous lessons | No | No | Yes | Analog signal |
Unit of learning and memory | PC | Microzone | PC | PC |
cf-trained learning at pf-MLI synapse | No | LTP | Yes, in different directions on outer and deeper level cells | Yes |
Learning algorithm | No | No | Yes | Yes—assumed criterion of system performance is the mean square error |
Physiological derivation of synaptic learning function | No function | Yes | No | No |
Output of the model | Single PC firing rate* |
Functionally indivisible (i) learning and (ii) behaviour of the circuit |
Single PC firing rate** | Single PC firing rate |
What codes PC firing? | pf rates: data packaged in single signals, as ‘codons’ | pf rates: data indivisibly coded in all input | pf synaptic weights | pf synaptic weights |
Plastic outcome coupled to training variables? | No proposed physiological or computational mechanism that sets weights | No | Yes | Yes |
PC-nuclear anatomical contact ‘rules’ | Outside cortex-only scope | Functional and integrated | Not included | Not included |
Nucleo-olivary feedback | Outside cortex-only scope | Functional and integrated | Not included | Not included |
Function of unknown patterns | None | Self-inhibition by the circuit of its own output | No unknown patterns | None: an effect of noise is eliminated by training |
What limits pattern memory capacity? | Inhibition must block a response to random patterns | Conceivably no limit | Ultimately, overlap causes classification errors | Pattern memory is not the function of learning |
Majority pf-PC synaptic ‘silence’ | Supports predicted synaptic modification | Supports predicted synaptic modification | At best, not supporting evidence | At best, not supporting evidence |
Recorded firing linearly codes behavioural parameters | Consistent with binary weights | Consistent with polarised weights | Problematic | Problematic |
*Marr assumes ‘that the central nervous system has a means of converting a signal in a Purkinje cell axon into’ a motor command [77 p.455]
**Albus briefly moots that heterogeneously trained PCs may code a motor sequence, but this does not form part of the model. The short section on firing of nuclear cells really only states in the form of mathematical symbols what inputs nuclear cells receive